Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06460740
Status:
RECRUITING
Last Update Posted:
2024-06-26
First Post:
2024-06-11
Brief Title:
Comb Effect of 4-7-8 Breathing Technique and Stationary Cycle on PP QOL and Dyspnea in Post CABG Patients
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Combined Effects of 4-7-8 Breathing Technique and Stationary Cycle on Physical Performance Quality of Life and Dyspnea in Post CABG Patients
Status:
RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To determine the combined effects of 4-7-8 breathing technique and stationary cycle on physical performance quality of life and dyspnea in post CABG patients
Detailed Description:
Patients who meet the inclusion criteria and will be excluded from the exclusion criteria will be recruited by convenient sampling technique and will be allocated to simple randomization process By taking a sample of 58 patients through non-probability convenience sampling and randomly assigning them into two groups Group A and Group B for 18 exercise sessions per month four to five times in a week out of which group A will receive 4-7-8 breathing technique and stationary cycle n29 Group B will alone receive Stationary cycle n29 The study will be Single-blind where patients will be only blind Pre and post treatment training outcomes of physical performance will be measured through 6-minute walk test quality of life will be measured through Short-item 36 SF-36 questionnaire 20 version and dyspnea will be measured through modified Borg scale The data will be analyzed through SPSS version 26 Generalized active range of motion will be given to both groups
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None